Canonical Allele Identifier:
CA1283487479
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.120331999C= , CM000664.2:g.120331999C= | GRCh38 |
| NC_000002.11:g.121089575C= , CM000664.1:g.121089575C= | GRCh37 |
| NC_000002.10:g.120806045C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011512307.1:c.141+3193C= | XP_011510609.1:n.141+3193C= |